参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 反应物 | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| 反应物 | 1-(叔丁氧基羰基)氮杂环丁烷-3-乙酸 | HCID 11095989 | — |
| 反应物 | N-(5-(N'-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 86677441 | — |
| 溶剂 | 甲基吡咯烷酮 | HCID 13387 | — |
| 产物 | Tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylate | HCID 71281398 | — |
反应步骤
Carbonyl diimidazole (CDI) (52.0 mg, 0.32 mmol) was added to a stirred solution of 2-(1-(tert-butoxycarbonyl)azetidin-3-yl)acetic acid (69.0 mg, 0.32 mmol) in NMP (1.0 mL). After 20 minutes, N-(5-(N′-hydroxycarbamimidoyl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (9) (49.5 mg, 0.16 mmol) was added in one portion and the resulting solution was stirred for 30 minutes before it was heated at 125° C. for 15 minutes in a microwave reactor. The reaction mixture was added dropwise to water (20 mL) with stirring. The precipitate was filtered and dried to give tert-butyl 3-((3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methyl)azetidine-1-carboxylate (54). MS m/z 489.2 (M+1)+.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US08754071B2 |
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| 来源数据集 | uspto-grants-2014_06 |
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| ORD ID | ord-6cdf3e92c7e2492dab844346282e1328 |
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| 来源说明 | uspto-grants-2014_06 |
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